Central Nervous System Part III Flashcards

1
Q

Define/differentiate concussion, contusion, subdural/subarachnoid hematoma, and cerebral edema.

A

Concussion: temporary alteration in brain function – typically following a blow to the head; repeated concussions can cause cumulative damage

Contusion: permanent damage caused by bruising of the brain

Subdural or Subarachnoid Hemorrhages: ruptured blood vessels bleed into these available spaces; pressure from the blood may compress the brain and cause sudden, neurological decline

Cerebral Edema: swelling of brain associated with traumatic head injury

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2
Q

What is ischemia? What is a cerebral vascular accident (CVA)? How do most CVAs occur?

A

Ischemia: any tissue deprived of blood supply - can lead to tissue death

Ischemia of brain tissue can be caused by blockage of a cerebral artery by a blood clot

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3
Q

Define hemiplegia. How do CVAs cause hemiplegia?

A

Hemiplegia - paralysis on one side of the body often caused by CVA – sensory and speech deficits may also occur

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4
Q

What is a TIA? What is TPA?

A

Transient Ischemia Attacks (TIA): temporary episodes of reversible cerebral ischemia; often a warning sign of a larger CVA

Tissue Plasminogen Activator (TPA) is the most effective treatment for acute stroke

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5
Q

Define Alzheimer’s Disease. What are some symptoms? What are 2 potential anatomical structures associated with Alzheimer’s Disease that cause neuronal death?

A

Alzheimer’s Disease (AD) - Progressive, degenerative disease of the brain that results in dementia

Symptoms - memory loss, short attention span, disorientation, eventual language loss, irritability, moodiness, confusion, and hallucinations

Neurofibrillary Tangles: formed from the protein tau inside the neurons; tangles interfere with the neuron’s transport mechanisms and eventually kill the neurons

The brain shrinks as neurons die

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6
Q

Define Parkinson Disease. What are some symptoms? What is a potential cause? What is a treatment?

A

Parkinson’s Disease - Degeneration of dopamine-releasing neurons of the substantia nigra

The basal nuclei deprived of dopamine become overactive – results in tremors

Overall cause is unknown, but theories exist about mitochondrial abnormalities or protein degradation pathways

Treatment: L-dopa (a dopamine precursor), deep brain stimulation, and gene therapy

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7
Q

Define Huntington Disease. What causes it? What are some symptoms? What is a potential treatment?

A

Huntington’s Disease

Fatal hereditary disorder caused by the accumulation of the protein huntingtin in brain cells – leads to degeneration of basal nuclei and the cerebral cortex

Onset is often in middle age
Initial symptoms: wild, jerky, “flapping”-like movements; followed by mental deterioration

“Chorea”: excessive, writhing movements; Greek for “dance”

Condition is typically fatal within 15 years

Treatment: drugs that block the effects of dopamine – stem cell implant research is promising

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8
Q

Where does the spinal cord begin? Where does it end?

A

The spinal cord begins at the foramen magnum and ends at the L1/L2 vertebra

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9
Q

What 2 functions does the spinal cord provide?

A

Provides 2-way communication between the brain and body

Acts as a major reflex center – reflexes are initiated and completed at the spinal cord

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10
Q

How is the spinal cord protected?

A

The spinal cord is protected by bone, meninges, and CSF

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11
Q

What can you find in the epidural space? What is the clinical importance of the epidural space?

A

Epidural Space - cushion of fat and a network of veins in the space between vertebrae and the spinal dura mater

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12
Q

What can you find in the subarachnoid space?

A

Subarachnoid Space - space between the arachnoid and pia maters; it is filled with CSF

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13
Q

Define and be ready to identify: conus medullaris, filum terminale, denticulate ligaments, cauda equina, ventral median fissure, dorsal median sulcus, and central canal.

A

The spinal cord terminates in a cone-shaped structure called the conus medullaris

Filum Terminale: a fibrous extension of the conus medullaris covered with pia mater. It extends to the coccyx and anchors the spinal cord.

Denticulate Ligaments: extensions of pia mater that secure the spinal cord to the dura mater

Cauda Equina: collection of nerve roots at the inferior end of the vertebral canal

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14
Q

Why are there cervical and lumbar enlargements in the spinal cord?

A

Cervical and Lumbar Enlargements - areas of the spinal cord where the nerves servicing the upper and lower limbs arise

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15
Q

Draw out how spinal nerves exist the spinal cord at each vertebral level.

A
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16
Q

The spinal cord’s central canal is filled with CSF, and it is continuous with the _______________.

A

brain’s 4th ventricle

17
Q

What are the 3 gray columns of the spinal cord? What is located in each column?

A

Dorsal Horns: interneurons that receive somatic and visceral sensory inputs

Ventral Horns: some interneurons, mostly somatic motor neurons

Lateral Horns: only exist in thoracic and superior lumbar regions; autonomic (sympathetic) neurons that innervate the visceral organs

18
Q

What is the gray commissure?

A

Gray Commissure: bridge of gray matter that connects the masses of gray matter on either side of the central canal

19
Q

Define, know the function of, and be ready to identify: ventral root, dorsal root, and spinal nerve.

A

Ventral Roots: bundle of motor neuron axons that exit the ventral spinal cord

Dorsal Roots: sensory inputs into the dorsal spinal cord

Dorsal Root (Spinal) Ganglion: cell bodies of the sensory neurons

Spinal Nerves: formed by the fusion of the dorsal and ventral roots

20
Q

Draw out how the spinal cord’s gray matter is divided into 4 groups.

A
21
Q

What are the 3 white funiculi of the spinal cord? What makes white matter white?

A

Dorsal (Posterior)
Lateral
Ventral (Anterior)

22
Q

What type of communication is happening with each direction of white fiber tract?

A

Ascending: up to the higher centers (sensory inputs)

Descending: from the brain to the spinal cord or to the lower cord levels (motor outputs)

Transverse: from 1 side of the spinal cord to the other (commissural fibers)

23
Q

The spinal cord is particularly sensitive to _____________________.

A

Direct pressure

24
Q

Define paresthesia and paralysis. What are the 2 types of paralysis?

A

Paresthesia: loss of sensory function; caused by damage to the dorsal roots or sensory tracts

Paralysis: loss of motor function; caused by damage to the ventral roots or ventral horn cells

2 Types: Flaccid or Spastic

Flaccid Paralysis: severe damage to the ventral root or ventral horn cells

  • Impulses do not reach the skeletal muscles
  • There is no voluntary or involuntary control of the muscles
  • Muscles atrophy secondary to disuse

Spastic Paralysis: damage to the upper motor neurons of the primary motor cortex or their axons in the spinal cord

  • Spinal more neurons remain intact; muscles are stimulated by reflexes
  • There is no voluntary control of muscles, only relfex
  • Muscles often shorten permanently (muscle contracture)
25
Q

Be ready to explain how each type of paralysis occurs and how you would expect it to look in a patient.

A

26
Q

Differentiate paraplegia and quadriplegia. Know (generally) what spinal cord level injuries are likely to result in these conditions.

A

Paraplegia: transection of the spinal cord between T1 and L1

Quadriplegia: transection of the spinal cord in the cervical region

27
Q

What is poliomyelitis? What causes it? What portion of the spinal cord is harmed? What are the short and long term symptoms?

A

Poliomyelitis

An epidemic in the late 1940s and 1950s – vaccine invented in 1952

Destruction of the ventral horn motor neurons by poliovirus

Symptoms: fever, headache, muscle pain and weakness, and loss of certain somatic reflexes

Muscles atrophy because of paralysis

Death can occur from paralysis of respiratory muscles or cardiac arrest

As a result of progressive neuron loss, survivors often develop postpolio syndrome years later

28
Q

What is ALS? What might cause it? What portion of the spinal cord is harmed? What is a potential treatment?

A

Amyotrophic Lateral Sclerosis (ALS)

Also called “Lou Gehrig’s Disease”

Destruction of ventral horn motor neurons and the fibers of the pyramidal tracts

Symptoms: loss of abilities to speak, swallow, and breathe

Death typically occurs within 5 years

Caused by the interaction of environmental factors and genetic mutations involving RNA processing

Treatment: only treatment is a drug that interferes with glutamate signaling called riluzole – glutamate is a neurotransmitter indicated as a potential cause of neuron death in a couple different conditions